Zr-labeled N4MU01 radioimmunoconjugates as theranostics against nectin-4 positive triple negative breast cancer
Hanan BabekeriD, Fabrice Ngoh NjotuiD, Jessica Pougoue KetchemeniD, Alissar MonzeriD, Anjong Florence TikumiD, Alireza DoroudiiD, Emmanuel NwangeleiD, Maruti UppalapatiiD, Humphrey FongeiD
Abstract
PurposeNectin-4 is an overexpressed biomarker in 60-70% of triple-negative breast cancer (TNBC), and an ideal target for radiotherapy and PET imaging. In this study, we have developed theranostic radioimmunoconjugates (RICs) based on a fully-human anti-nectin-4 antibody, N4MU01. We characterized and evaluated the efficacy of these RICs for applications in molecular imaging and radiotherapy of aggressive TNBC models. MethodsAn anti-nectin-4 antibody (N4MU01) was radiolabeled with 89Zr and 225Ac, for imaging and radiotherapy, respectively, using TNBC xenograft and syngeneic models. Biodistribution & PET imaging of [89Zr]Zr-DFO-N4MU01 RIC was studied in mice bearing nectin-4 positive xenografts. Dosimetry of [225Ac]Ac-Macropa-N4MU01 was studied in healthy mice, and therapeutic efficacy was evaluated in mice bearing human TNBC MDA-MB-468 xenograft and in a syngeneic xenograft model using murine 4T1 breast cancer cells transfected with human nectin-4 (4T1.nectin-4). Mice received 2 doses of 13 kBq or 18.6 kBq 10 days apart. ResultsThe pharmacokinetic profile of [89Zr]Zr-DFO-N4MU01 RIC showed biphasic distribution with a moderate elimination half-life of 63 h. PET imaging and biodistribution of [89Zr]Zr-DFO-N4MU01 in mice bearing MDA-MB-468 xenograft showed high tumor uptake of 13.2 {+/-} 1.12 %IA/g at 120 h. [225Ac]Ac-Macropa-N4MU01 was effectively internalized in MDA-MB-468 and was cytotoxic to the cells with IC50 of 1.2 kBq/mL. Mice bearing MDA-MB-468 xenograft treated with [225Ac]Ac-Macropa-N4MU01 (13 kBq or 18.6 kBq) had a remarkable tumor growth inhibition that was dose dependent. For the syngeneic 4T1.nectin-4 model, treatment with [225Ac]Ac-Macropa-N4MU01 (13 kBq) led to complete tumor remission in 83.3% (5/6) of mice. ConclusionThe specific tumor uptake and remarkable effectiveness at shrinking aggressive TNBC tumors is very promising towards clinical development of N4MU01 RICs as theranostics against TNBC.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 20
- FWCI
- 8.18
- Field percentile
- top 1%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- IL-4 receptor targeting as an effective immunotherapy against triple-negative breast cancer
S. Parveen, S. Siddharth, … W. R. Bishai·bioRxiv·Aug 5, 2020
- Neoadjuvant anti-4-1BB confers protection against spontaneous metastasis through low-affinity intratumor CD8+ T cells in triple-negative breast cancer
Bryan Jian Wei Lim, Mingyong Liu, … Qi-Jing Li·bioRxiv·Jan 29, 2025
- Tumor microenvironment immunomodulation by nanoformulated TLR 7/8 agonist and PI3k delta inhibitor enhances therapeutic benefits of radiotherapy
Mostafa Yazdimamaghani, Oleg V. Kolupaev, … Jonathan Stuart Serody·BiomaterialsPeer-reviewed·Aug 8, 2024
- Development of metastases in mice induced by plasma sample collected during radiotherapy in patient with triple-negative breast cancer: Role of Rab4A
Benoît Paquette, Hélène Therriault, … Jean‐Luc Parent·bioRxiv·Jul 23, 2025
- DNA-functionalized Gold Nanorods for Targeted Triple-modal Optical Imaging and Photothermal Therapy of Triple-negative Breast Cancer
S. Pal, J. K. Koneru, … J. Mondal·bioRxiv·Feb 12, 2022
- "Double-Effect" strategy against Triple-Negative Breast Cancer via a synergistic therapy of Magneto-mechanical Force enhancing NIR-II Hypothermal Ablation